Canonical Allele Identifier: CA2634928150

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153680-C-CGGGCCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153680_89153681insGGGCCAG , CM000678.2:g.89153680_89153681insGGGCCAG	GRCh38
NC_000016.9:g.89220088_89220089insGGGCCAG , CM000678.1:g.89220088_89220089insGGGCCAG	GRCh37
NC_000016.8:g.87747589_87747590insGGGCCAG	NCBI36
NG_031961.1:g.64872_64873insGGGCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-410_1614-409insGGGCCAG	ENSP00000320646.4:n.1614-410_1614-409insGGGCCAG
ENST00000614302.5:c.1614-410_1614-409insGGGCCAG MANE Select	ENSP00000479130.1:n.1614-410_1614-409insGGGCCAG
ENST00000649953.1:c.1824-410_1824-409insGGGCCAG	ENSP00000497456.1:n.1824-410_1824-409insGGGCCAG
ENST00000317447.8:c.1614-410_1614-409insGGGCCAG	ENSP00000320646.4:n.1614-410_1614-409insGGGCCAG
ENST00000378345.8:c.819-410_819-409insGGGCCAG	ENSP00000367596.4:n.819-410_819-409insGGGCCAG
ENST00000393145.5:n.6114_6115insGGGCCAG
ENST00000406948.7:c.1614-410_1614-409insGGGCCAG	ENSP00000384627.3:n.1614-410_1614-409insGGGCCAG
ENST00000537116.5:n.740-410_740-409insGGGCCAG
ENST00000537155.1:n.354-410_354-409insGGGCCAG
ENST00000542688.5:c.*358-410_*358-409insGGGCCAG	ENSP00000446281.1:n.*358-410_*358-409insGGGCCAG
ENST00000614302.4:c.1614-410_1614-409insGGGCCAG	ENSP00000479130.1:n.1614-410_1614-409insGGGCCAG
NM_001127214.3:c.1614-410_1614-409insGGGCCAG	NP_001120686.1:n.1614-410_1614-409insGGGCCAG
NM_001243279.2:c.1614-410_1614-409insGGGCCAG	NP_001230208.1:n.1614-410_1614-409insGGGCCAG
NM_001284316.1:c.819-410_819-409insGGGCCAG	NP_001271245.1:n.819-410_819-409insGGGCCAG
NM_174917.4:c.1614-410_1614-409insGGGCCAG	NP_777577.2:n.1614-410_1614-409insGGGCCAG
NR_045667.2:n.740-410_740-409insGGGCCAG
NR_104293.1:n.2048-410_2048-409insGGGCCAG
XR_933239.1:n.2055-410_2055-409insGGGCCAG
XR_933240.1:n.2052-410_2052-409insGGGCCAG
XR_933241.1:n.1809-410_1809-409insGGGCCAG
NR_147928.1:n.2092-410_2092-409insGGGCCAG
NR_147929.1:n.1846-410_1846-409insGGGCCAG
XM_017023020.2:c.-3491-410_-3491-409insGGGCCAG	XP_016878509.1:n.-3491-410_-3491-409insGGGCCAG
XM_024450187.1:c.819-410_819-409insGGGCCAG	XP_024305955.1:n.819-410_819-409insGGGCCAG
XR_001751864.2:n.1861-410_1861-409insGGGCCAG
XR_933240.3:n.2051-410_2051-409insGGGCCAG
NM_001127214.4:c.1614-410_1614-409insGGGCCAG	NP_001120686.1:n.1614-410_1614-409insGGGCCAG
NM_001243279.3:c.1614-410_1614-409insGGGCCAG MANE Select	NP_001230208.1:n.1614-410_1614-409insGGGCCAG
NM_001284316.2:c.819-410_819-409insGGGCCAG	NP_001271245.1:n.819-410_819-409insGGGCCAG
NM_174917.5:c.1614-410_1614-409insGGGCCAG	NP_777577.2:n.1614-410_1614-409insGGGCCAG
NR_104293.2:n.2005-410_2005-409insGGGCCAG
NR_147928.2:n.2049-410_2049-409insGGGCCAG
NR_147929.2:n.1803-410_1803-409insGGGCCAG